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435 results

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Page 1
COG6-CDG: Novel variants and novel malformation.
Cirnigliaro L, Bianchi P, Sturiale L, Garozzo D, Mangili G, Keldermans L, Rizzo R, Matthijs G, Fiumara A, Jaeken J, Barone R. Cirnigliaro L, et al. Among authors: jaeken j. Birth Defects Res. 2022 Mar;114(5-6):165-174. doi: 10.1002/bdr2.1981. Epub 2022 Jan 23. Birth Defects Res. 2022. PMID: 35068072 Free PMC article.
COG5-CDG: expanding the clinical spectrum.
Rymen D, Keldermans L, Race V, Régal L, Deconinck N, Dionisi-Vici C, Fung CW, Sturiale L, Rosnoblet C, Foulquier F, Matthijs G, Jaeken J. Rymen D, et al. Among authors: jaeken j. Orphanet J Rare Dis. 2012 Dec 10;7:94. doi: 10.1186/1750-1172-7-94. Orphanet J Rare Dis. 2012. PMID: 23228021 Free PMC article.
ALG12-CDG: novel glycophenotype insights endorse the molecular defect.
Sturiale L, Bianca S, Garozzo D, Terracciano A, Agolini E, Messina A, Palmigiano A, Esposito F, Barone C, Novelli A, Fiumara A, Jaeken J, Barone R. Sturiale L, et al. Among authors: jaeken j. Glycoconj J. 2019 Dec;36(6):461-472. doi: 10.1007/s10719-019-09890-2. Epub 2019 Sep 16. Glycoconj J. 2019. PMID: 31529350
MAN1B1-CDG: novel patients and novel variant.
Kasapkara CS, Olgac A, Kilic M, Keldermans L, Matthijs G, Jaeken J. Kasapkara CS, et al. Among authors: jaeken j. J Pediatr Endocrinol Metab. 2021 Jun 24;34(9):1207-1209. doi: 10.1515/jpem-2021-0038. Print 2021 Sep 27. J Pediatr Endocrinol Metab. 2021. PMID: 34162022
CDG or not CDG.
Freeze HH, Jaeken J, Matthijs G. Freeze HH, et al. Among authors: jaeken j. J Inherit Metab Dis. 2022 May;45(3):383-385. doi: 10.1002/jimd.12498. Epub 2022 Apr 1. J Inherit Metab Dis. 2022. PMID: 35338706 Free PMC article. No abstract available.
A new mutation in COG7 extends the spectrum of COG subunit deficiencies.
Zeevaert R, Foulquier F, Cheillan D, Cloix I, Guffon N, Sturiale L, Garozzo D, Matthijs G, Jaeken J. Zeevaert R, et al. Among authors: jaeken j. Eur J Med Genet. 2009 Sep-Oct;52(5):303-5. doi: 10.1016/j.ejmg.2009.06.006. Epub 2009 Jul 3. Eur J Med Genet. 2009. PMID: 19577670
From glycosylation to glycosylation diseases.
Jaeken J, Matthijs G. Jaeken J, et al. Biochim Biophys Acta. 2009 Sep;1792(9):823. doi: 10.1016/j.bbadis.2009.08.003. Biochim Biophys Acta. 2009. PMID: 19765533 Free article. No abstract available.
CDG nomenclature: time for a change!
Jaeken J, Hennet T, Matthijs G, Freeze HH. Jaeken J, et al. Biochim Biophys Acta. 2009 Sep;1792(9):825-6. doi: 10.1016/j.bbadis.2009.08.005. Biochim Biophys Acta. 2009. PMID: 19765534 Free PMC article. No abstract available.
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy.
Barone R, Aiello C, Race V, Morava E, Foulquier F, Riemersma M, Passarelli C, Concolino D, Carella M, Santorelli F, Vleugels W, Mercuri E, Garozzo D, Sturiale L, Messina S, Jaeken J, Fiumara A, Wevers RA, Bertini E, Matthijs G, Lefeber DJ. Barone R, et al. Among authors: jaeken j. Ann Neurol. 2012 Oct;72(4):550-8. doi: 10.1002/ana.23632. Ann Neurol. 2012. PMID: 23109149
435 results